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经验公式(希尔记法):
C10H16O4S
化学文摘社编号:
分子量:
232.30
UNSPSC Code:
12352115
NACRES:
NA.22
PubChem Substance ID:
EC Number:
252-817-9
Beilstein/REAXYS Number:
2809676
MDL number:
产品名称
(-)-樟脑-10-磺酸, purum, ≥98.0% (T)
InChI key
MIOPJNTWMNEORI-XVKPBYJWSA-N
InChI
1S/C10H16O4S/c1-9(2)7-3-4-10(9,8(11)5-7)6-15(12,13)14/h7H,3-6H2,1-2H3,(H,12,13,14)/t7-,10-/m0/s1
SMILES string
CC1(C)C2CC[C@]1(CS(O)(=O)=O)C(=O)C2
grade
purum
assay
≥98.0% (T)
optical activity
[α]20/D −21.5±1°, c = 10% in H2O
functional group
ketone
sulfonic acid
Quality Level
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可能含一些深色颗粒
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Ruizhi Pang et al.
Journal of colloid and interface science, 510, 127-132 (2017-09-25)
Thin film nanocomposite reverse osmosis (TFN RO) membranes incorporated with hydrophilic nanoparticles show a potential problem that the salt rejection can not be improved significantly. In this study, novel TFN RO membranes incorporated with hydrophobic fluorinated silica nanoparticles were fabricated
Chen Liu et al.
Organic letters, 13(10), 2638-2641 (2011-04-23)
A novel ion pair catalyst containing a chiral counteranion can be readily derived by simply mixing cinchona alkaloid-derived diamine with chiral camphorsulfonic acid (CSA). A mixture of 9-amino(9-deoxy)epi-quinine 8 and (-)-CSA was found to be the best catalyst with matching
Bala Kishan Gorityala et al.
Bioorganic & medicinal chemistry letters, 19(11), 3093-3095 (2009-04-29)
A mild and efficient synthesis of pseudoglycosides has been developed using metal free (S)-camphorsulfonic acid. (S)-CSA acts as an excellent catalyst for conversion of 2,4,6-tri-O-acetyl-D-glucal to 2,3-unsaturated O-glycosides. A wide range of biologically active natural products, alcohols and thiols could
Chen Liu et al.
Organic letters, 12(10), 2278-2281 (2010-04-24)
The combination of 9-amino-9-deoxy-epi-cinchonine and (+)-CSA resulted in a novel primary amine-based organocatalyst for effective iminium activation of alpha,beta-unsaturated ketones. Such a catalytic system could catalyze the conjugate addition of nitroacetate to enones in a highly enantioselective manner, affording the
Anne-Catherine Servais et al.
Electrophoresis, 25(16), 2701-2710 (2004-09-08)
The enantiomeric separation of a series of basic pharmaceuticals (beta-blockers, local anesthetics, sympathomimetics) has been investigated in nonaqueous capillary electrophoresis (NACE) systems using heptakis(2,3-di-O-methyl-6-O-sulfo)-beta-cyclodextrin (HDMS-beta-CD) in combination with potassium camphorsulfonate (camphorSO3-). For this purpose, a face-centered central composite design with
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